Director – Clinical Scientist
Posted on 3/22/2024
INACTIVE
Verve Therapeutics

201-500 employees

Develops gene editing therapies for heart disease
Company Overview
Verve Therapeutics, a clinical-stage biotechnology company, is a leading player in the fight against heart disease, leveraging its expertise in cardiovascular medicine, human genetics, and gene editing to develop transformative, once-and-done therapies. The company's unique approach to gene editing, designed to permanently lower LDL cholesterol and triglyceride levels, sets it apart from competitors and positions it at the forefront of precision genetic medicine. With a culture that fosters passion and drive, Verve has been recognized as a "Best Places to Work" by the Boston Globe, demonstrating its commitment to both its mission and its employees.
Biotechnology

Company Stage

N/A

Total Funding

$419.3M

Founded

2018

Headquarters

Boston, Massachusetts

Growth & Insights
Headcount

6 month growth

3%

1 year growth

14%

2 year growth

94%
Locations
Cambridge, MA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Communications
CategoriesNew
Medical, Clinical & Veterinary
Healthcare Administration & Support
Physicians & Surgeons
Requirements
  • Advanced degree in life sciences (PhD, MD or both)
  • Experience with the development of key clinical study documents
  • Experience with the analysis and review of clinical data
  • Working knowledge of biostatistics, GCP, and regulatory requirements for clinical studies
  • Track record of working with and managing CROs and external vendors
  • Strong attention to detail and organizational skills
  • Exceptional verbal and written communication skills
  • Ability to build strong relationships and work effectively with cross-functional teams
Responsibilities
  • Review, analyze, and interpret emerging clinical trial data
  • Lead preparation for key study meetings
  • Partnership with the medical monitor on oversight of clinical trial activities
  • Liaison role with the broader clinical development team
  • Contribution to authoring key study and regulatory documents
  • Leadership in internal meetings and review topics
  • Collaborate with clinical and research teams to implement the clinical biomarker strategy
  • Ensuring compliance with ICH/GCP guidelines and applicable regulatory requirements
  • Contribution to the development of presentations, abstracts, and publications
  • Other duties as assigned